Abstract
Objective. This study investigated whether painful physical symptoms (PPSs) influenced quality of life (QoL) when adjusting for severity of depression. Methods. Severity of depression, QoL and PPSs were assessed at baseline and 3 months among the Chinese cohort (n = 300) of a 3-month observational study of major depressive disorder (MDD) in East Asia. The presence of PPS was defined as ‘a mean score of ≥2 on the Somatic Symptom Inventory pain-related items’. Regression analyses determined predictors of QoL at 3 months, adjusting for age, sex, depressive symptoms, overall severity and QoL at baseline. Results. PPSs were present (PPS+) at baseline in 35.3% of patients. Over 3 months, in the whole sample, EuroQoL visual analogue scale (EQ-VAS) score improved from 45.5 (standard deviation [SD]: 20.9) to 81 (SD: 16.7), and EuroQoL 5-Dimension Questionnaire (EQ-5D) score improved from 0.52 (SD: 0.31) to 0.89 (0.16). At 3 months, mean EQ-VAS was 75.9 (SD: 17.7) for PPS+ versus 83.7 (SD: 15.6) for PPS−, and mean EQ-5D was 0.83 (SD: 0.17) versus 0.92 (SD: 0.14). PPS+ at baseline was a significant predictor of QoL at 3 months after adjusting for socio-demographic and baseline clinical variables. Conclusions. PPSs were associated with less improvement in QoL in patients receiving treatment for MDD, independent of severity of depression.
Acknowledgements
The authors thank all of the investigators and patients in the study, and Sarah Smith PhD, for editorial assistance.
Statement of interest
This study (FIJ-AA-B015) was funded by Eli Lilly and Company, Indianapolis, USA. Disclosure: Diego Novick, William Montgomery and Xiaomei Peng are employees of Eli Lilly and Company. Maria Victoria Moneta has conducted the statistical analysis under a contract of Fundació Sant Joan de Deú with Eli Lilly and Co. Josep Maria Haro has acted as consultant or speaker for Astra-Zeneca, Eli Lilly and Co., Lundbeck and Roche.